La sindrome di Ehlers-Danlos. Descrizione di due casi clinici.

Translated title of the contribution: Ehlers-Danlos syndrome. Description of 2 clinical cases

A. Ottolini, A. Berardinelli, D. Besana, G. Cetta, K. M. Dyne, G. Lanzi

Research output: Contribution to journalArticlepeer-review


The paper describes the clinical symptoms and biochemical tests carried out in two girls suffering from Ehlers-Danlos syndrome. The most typical clinical feature, which is common to both cases, was the presence of skin alterations at the extensor surface level of elbows and, above all, knees. These alterations appeared to be delimited areas with irregular margins where the skin was thin, dry, hyperpigmented, wrinkled, with scanty or absent subcutaneous tissue. Biochemical tests carried out on cutaneous fibroblast cultures excluded the presence type I collagen alterations and an altered secretion of type I or III procollagen secretion. The Authors discuss the attribution of cases presented within the context of the various forms of Ehlers-Danlos syndrome in relation to clinical findings and the results of the biochemical tests.

Translated title of the contributionEhlers-Danlos syndrome. Description of 2 clinical cases
Original languageItalian
Pages (from-to)231-236
Number of pages6
JournalMinerva Pediatrica
Issue number5
Publication statusPublished - May 1992

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health


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